A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv15n100



Internal ID20151631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8992095..9056684hg38UCSC Ensembl
chr1:9052154..9116743hg19UCSC Ensembl
chr1:8974741..9039330hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3864590
hg1964590
hg1864590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005347, nsv1009990
Samples
Known GenesSLC2A5, SLC2A7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv15n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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